Hemoglobin, Volume 29, Issue 1 (2005)

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Hemoglobin, Volume 29, Issue 1 (2005)

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Original Article

Article
Hb Kochi [β141(H19)Leu→Val (g.1404 C→G); 144–146(HC1-3)Lys-Tyr-His→0 (g.1413 A→T)]: A New Variant with Increased Oxygen Affinity
Ayako Miyazaki, Toyofumi Nakanishi, Akira Shimizu M.D., Miki Mizobuchi, Yasuhiro Yamada & Kiyohiro Imai
Pages: 1-10
Published online: 07 Jul 2009
AbstractforHb Kochi [β141(H19)Leu→Val (g.1404 C→G); 144–146(HC1-3)Lys-Tyr-His→0 (g.1413 A→T)]: A New Variant with Increased Oxygen Affinity | Full Text | References | PDF (298.9 KB)
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Article
Hb Zoeterwoude [β23(B5)Val → Ala)]: A New β-Globin Variant Found in Association with Erythrocytosis
Cornelis L Harteveld Ph.D., J.H Marc Groeneveld, Bastiaan van Dam, Peter Van Delft, Nicole Akkerman, Sandra Arkesteijn & Piero C. Giordano
Pages: 11-17
Published online: 07 Jul 2009
AbstractforHb Zoeterwoude [β23(B5)Val → Ala)]: A New β-Globin Variant Found in Association with Erythrocytosis | Full Text | References | PDF (89 KB)
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Article
Hb Showa-Yakushiji [β110(G12)Leu→Pro] in Four Unrelated Patients from West Bengal
Eunice S. Edison, Ramachandran V. Shaji, Sankari G. Devi, Satheesh S. Kumar, Alok Srivastava & Mammen Chandy
Pages: 19-25
Published online: 07 Jul 2009
AbstractforHb Showa-Yakushiji [β110(G12)Leu→Pro] in Four Unrelated Patients from West Bengal | Full Text | References | PDF (165 KB)
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Article
Oxidative Reactions of Normal and Abnormal Hemoglobins in the Presence of Phosphatidylserine Vesicles
Merita Nirmali Dias Wickramaratne & Leslie Wo-Mei Fung
Pages: 27-42
Published online: 07 Jul 2009
AbstractforOxidative Reactions of Normal and Abnormal Hemoglobins in the Presence of Phosphatidylserine Vesicles | Full Text | References | PDF (373.9 KB)
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Article
Molecular Basis of Hb H Disease in Southwest Iran
Majid Yavarian, Mehran Karimi, Amine Zorai, Cornelis L Harteveld & Piero C Giordano
Pages: 43-50
Published online: 07 Jul 2009
AbstractforMolecular Basis of Hb H Disease in Southwest Iran | Full Text | References | PDF (87.7 KB)
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Article
Prevalence of α-Globin Gene Deletions Among Patients with Unexplained Microcytosis in a North-American Population
Julie Bergeron, Xiaoduan Weng, Louise Robin, Harold J Olney & Denis Soulières M.Sc.M.D.
Pages: 51-60
Published online: 07 Jul 2009
AbstractforPrevalence of α-Globin Gene Deletions Among Patients with Unexplained Microcytosis in a North-American Population | Full Text | References | PDF (88.5 KB)
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Short Communication

Article
Hb Riccarton [α51(CE9)Gly→Ser]: A Variant Arising from a Novel Mutation in the α1 Gene
Stephen O Brennan, Tim Chan, Mary Obele & Peter M George
Pages: 61-64
Published online: 07 Jul 2009
AbstractforHb Riccarton [α51(CE9)Gly→Ser]: A Variant Arising from a Novel Mutation in the α1 Gene | Full Text | References | PDF (105.2 KB)
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Article
Hb Tak: A β Chain Elongation at the End of the β Chain, in a Taiwanese
Mu-Chin Shih, Kang-His Wu, Su-Ching Liu & Jan-Gowth Chang M.D.
Pages: 65-67
Published online: 07 Jul 2009
AbstractforHb Tak: A β Chain Elongation at the End of the β Chain, in a Taiwanese | Full Text | References | PDF (247.2 KB)
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Article
Two New Hemoglobin Variants: Hb Brem-Sur-Mer [β9(A6)Ser→Tyr] and Hb Passy [α81(F2)Ser→Pro (α2)]
Philippe Lacan, Mathieu Moreau, Michel Becchi, Isabelle Zanella-Cleon, Martine Aubry, Jean-Jacques Louis, Nicole Couprie & Alain Francina
Pages: 69-75
Published online: 07 Jul 2009
AbstractforTwo New Hemoglobin Variants: Hb Brem-Sur-Mer [β9(A6)Ser→Tyr] and Hb Passy [α81(F2)Ser→Pro (α2)] | Full Text | References | PDF (294.4 KB)
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Article
Thalassemia Intermedia Associated with Complex Interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a Deletional α-Thalassemia-1 in a Thai Family
Supan Fucharoen, Sunisa Chunpanich, Kanokwan Sanchaisuriya, Goonnapa Fucharoen & Naowarat Kunyanone
Pages: 77-83
Published online: 07 Jul 2009
AbstractforThalassemia Intermedia Associated with Complex Interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a Deletional α-Thalassemia-1 in a Thai Family | Full Text | References | PDF (246.4 KB)
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Article
DNAase I Hypersensitive Site 3′ to the β-Globin Gene Cluster Containing Two TAA Insertions and a G→A Polymorphism is Predominantly Associated with the β+-Thalassemia IVS-I-6 (T→C) Mutation
Juliana T. N Martins, Silvana Bordin, Dulcinéia M. de Albuquerque, Sara T. O Saad & Fernando F. Costa
Pages: 85-89
Published online: 07 Jul 2009
AbstractforDNAase I Hypersensitive Site 3′ to the β-Globin Gene Cluster Containing Two TAA Insertions and a G→A Polymorphism is Predominantly Associated with the β+-Thalassemia IVS-I-6 (T→C) Mutation | Full Text | References | PDF (211.7 KB)
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